Boosting CO chemical fixation over MOF-808 by the introduction of functional groups and defective Zr sites
CO 2 cycloaddition has emerged as a promising approach for producing value-added cyclocarbonates and mitigating greenhouse gas emissions. Although MOF-808 serves as a stable catalyst for cycloaddition, its limited activity constrains broader applications. Through the modification with a fluoride gro...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2024-03, Vol.6 (23), p.317-3173 |
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Zusammenfassung: | CO
2
cycloaddition has emerged as a promising approach for producing value-added cyclocarbonates and mitigating greenhouse gas emissions. Although MOF-808 serves as a stable catalyst for cycloaddition, its limited activity constrains broader applications. Through the modification with a fluoride group
via
a ligand exchange method, F-MOF-808-1.5 exhibits exceptional performance, achieving a 98.8% conversion with 97.8% selectivity to epichlorohydrin carbonate-marking a substantial 100% improvement compared to pristine MOF-808. The defective Zr sites and the electron-withdrawing groups synergistically promote the ring opening of epoxides. Furthermore, the catalyst demonstrates high stability over multiple reaction cycles. Notably, without adding solvents and co-catalysts, F-MOF-808-1.5 outperforms most reported MOF-based catalysts.
F-MOF-808, prepared
via
ligand exchange, exhibit an optimized electronic structure and sufficient defective Zr sites, thus excelling in CO
2
cycloaddition with a 100% enhancement over the original MOF-808 and maintaining high activity through 6 runs. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/d3cc06154j |